CARESCAPE Central StationRecalls & reported problems across all models

We found 4 models of CARESCAPE Central Station by Ge Medical Systems Information Technologies, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Feb 2, 2026 and Feb 2, 2026 — classified as 1 death.

The most frequently reported specific device problem is “No Audible Alarm” (1 report).

6 FDA recall records name at least one of these models by its device identifier, 5 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

CARESCAPE Central Station recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Jul 30, 2026Open, Classified

   Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.

   Z-3143-2026 · Root cause: Under Investigation by firm · names 2 of these models · Recall details · FDA record ↗

2. Sep 5, 2025Open, Classified

   Carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs only when the number of central stations connected to the network is 118, 119 or 120.

   Z-0214-2026 · Root cause: Software design · names 2 of these models · Recall details · FDA record ↗

3. Sep 5, 2025Open, Classified

   Carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs only when the number of central stations connected to the network is 118, 119 or 120.

   Z-0213-2026 · Root cause: Software design · Recall details · FDA record ↗

4. May 10, 2022Open, Classified

   The CARESAPE Central Station (CSCS) V2 can shut down due to a potential power supply component failure. This can lead to loss of patient monitoring at the central station.

   Z-1265-2022 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗

5. Jan 28, 2022Open, Classified

   If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard, the audio can be muted resulting in loss of audible alarms.

   Z-0808-2022 · Root cause: Software design · names 2 of these models · Recall details · FDA record ↗

6. Jan 11, 2018Terminated

   CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience unexpected NO COMM (No Communication) and network communication issues after boot-up or system restart.

   Z-0487-2018 · Root cause: Software in the Use Environment · names 2 of these models · Recall details · FDA record ↗

Most reported CARESCAPE Central Station problems

CARESCAPE Central Station models

4 models, most reported first. Each model has its own page with its reports, recalls and device details.

• CARESCAPE CENTRAL STATION MAI800

  Computer, Diagnostic, Programmable
  3 recalls0 reports
• CARESCAPE Central Station V2 Standard MAS 700

  DETECTOR AND ALARM, ARRHYTHMIA
  3 recalls0 reports
• CARESCAPE Central Station V2 Integrated MAI 700

  DETECTOR AND ALARM, ARRHYTHMIA
  3 recalls0 reports
• CARESCAPE CENTRAL STATION MAI800

  Computer, Diagnostic, Programmable
  2 recalls1 death1 report

Recent CARESCAPE Central Station adverse event reports

The 1 most recent reports across all models, in the reporter's own words as published by the FDA.

• DeathFeb 2, 2026No Audible Alarm

  IT WAS REPORTED THAT A PATIENT WAS FOUND UNRESPONSIVE AND THE CENTRAL STATION MAY NOT HAVE AUDIBLY ALARMED. THE PATIENT WAS TRANSFERRED TO THE ICU WHERE THEY EVENTUALLY EXPIRED.

  Patient problems: Insufficient Information

  MAUDE report 24240085 ↗

Other Ge Medical Systems Information Technologies, Inc. products

• MAC4 models · 1 reports · 4 recalls
• CARESCAPE3 models · 3 reports · 2 recalls
• ONE-CUF12 models · 1 reports · 1 recall
• CARESCAPE ONE2 models · 0 reports · 1 recall